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The Journal of Chemical Physics

Observation of infrared free-induction decay and optical nutation signals from nitrous oxide using a current modulated quantum cascade laser

GEOFFREY DUXBURY, James Floyd Kelly, Thomas A. Blake, Nigel Langford

Published May 7, 2012• 8 citations
Publisher

Abstract

Free induction decay (FID), optical nutation, and rapid passage induced signals in nitrous oxide, under both optically thin and optically thick conditions, have been observed using a rapid current pulse modulation, or chirp, applied to the slow current ramp of a quantum cascade (QC) laser. The variation in optical depth was achieved by increasing the pressure of nitrous oxide in a long path length multipass absorption cell. This allows the variation of optical depth to be achieved over a range of low gas pressures. Since, even at the highest gas pressure used in the cell, the chirp rate of the QC laser is faster than the collisional reorientation time of the molecules, there is minimal collisional damping, allowing a large macroscopic polarization of the molecular dipoles to develop. This is referred to as rapid passage induced polarization. The resultant FID signals are enhanced due to the constructive interference between the field within the gas generated by the slow ramp of the laser (pump), and that of the fast chirp of the laser (probe) signal generated by pulse modulation of the continuously operating QC laser. The FID signals obtained at large optical depth have not been observed previously in the mid-infrared regions, and unusual oscillatory signals have been observed at the highest gas pressures used.

DOI
10.1063/1.4710540

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Free induction decay (FID), optical nutation, and rapid passage induced signals in nitrous oxide, under both optically thin and optically thick conditions, have been observed using a rapid current pulse modulation, or chirp, applied to the slow current ramp of a quantum cascade (QC) laser. The variation in optical depth was achieved by increasing the pressure of nitrous oxide in a long path length multipass absorption cell. This allows the variation of optical depth to be achieved over a range of low gas pressures. Since, even at the highest gas pressure used in the cell, the chirp rate of the QC laser is faster than the collisional reorientation time of the molecules, there is minimal collisional damping, allowing a large macroscopic polarization of the molecular dipoles to develop. This is referred to as rapid passage induced polarization. The resultant FID signals are enhanced due to the constructive interference between the field within the gas generated by the slow ramp of the laser (pump), and that of the fast chirp of the laser (probe) signal generated by pulse modulation of the continuously operating QC laser. The FID signals obtained at large optical depth have not been observed previously in the mid-infrared regions, and unusual oscillatory signals have been observed at the highest gas pressures used.
Using a low power, rapid (nsec) pulse-modulated quantum cascade (QC) laser, collective coherent effects in the 5 μm spectrum of nitric oxide have been demonstrated by the observation of sub-Doppler hyperfine splitting and also Autler-Townes splitting of Doppler broadened lines. For nitrous oxide, experiments and model calculations have demonstrated that two main effects occur with pulse-modulated (chirped) quantum cascade lasers: free induction decay signals, and signals induced by rapid passage during the laser chirp. In the open shell molecule, NO, in which both Λ-doubling splitting and hyperfine structure occur, laser field-induced coupling between the hyperfine levels of the two Λ-doublet components can induce a large ac Stark effect. This may be observed as sub-Doppler structure, field-induced splittings, or Autler-Townes splitting of a Doppler broadened line. These represent an extension of the types of behaviour observed in the closed shell molecule nitrous oxide, using the same apparatus, when probed with an 8 μm QC laser.
Rapid passage signals showing the effects of molecular alignment have been observed when low pressure samples of nitrous oxide are interrogated by radiation from a pulsed 7.84 µm quantum cascade laser. These effects occur when the sweep rate of the laser through a Doppler broadened absorption line is much faster than the collisional relaxation time, and when the power density of the linearly polarized laser radiation is sufficient to cause optical pumping. Using a laser pulse of duration 1.3 µs, the frequency sweeps approximately 90 GHz. The variation of the laser tuning rate during the laser pulse, from about100 MHz/ns at the beginning to about 20 MHz/ns at the end, allows the relationship between sweep rate and collisional damping to be investigated. It is shown, by comparing the experimental signals with those calculated by coupled Maxwell–Bloch equations, how the rapid passage effects in nitrous oxide are influenced by the number density, transition cross-section and reorientation lifetime.
Rapid passage signals have been observed in which a delayed switch from absorption to emission is observed as the optical density of acetylene in a long path length cell is increased. The delayed switch results in the generation of a large, narrow, transient gain signal. Using numerical solutions of the Maxwell–Bloch equations we have demonstrated that this effect is due to constructive interference between the incident laser field and the field generated by the response of the gaseous medium. This occurs owing to the minimal collisional damping at the low gas pressures within the gas cell, so that the chirp rate of the laser is faster than the collisional reorientation time of the molecules.
In this Letter, a 10 microm quantum cascade laser operating in the intrapulse mode is used observe rapid passage (RP) effects within a 40 cm single-pass gas cell containing low pressures of NH(3). The laser tuning range allows the rotational states J=2 with K=0, 1, and 2 to be probed. We show that the RP structures change as a function of optical density and that the magnitude of the delay in the switch from absorption to emission as a function of increased gas pressure is dependent upon the initial value of K. These measurements are qualitatively well modeled using the Maxwell-Bloch equations.
Two 5 µm continuous wave quantum cascade lasers are used to perform a counterpropagating pump and probe experiment on a low pressure sample of nitric oxide. The strong pump field excites a fundamental rovibrational transition and the weaker probe field is tuned to the corresponding rotationally resolved hot band transition. When both light fields are in resonance, rapid passage is observed in the hot band absorption lineshape arising from a minimally damped and velocity-selected sample of molecules in the v=1 state. The measured rapid passage signals are well described by a two-level model based on the optical Bloch equations.